Eur J Appl Physiol. 2007 Feb;99(3):217-26. Epub 2006 Nov 11. Effects of adaptive exercise on apoptosis in cells of rat renal tubuli. Podhorska-Okolow M, Dziegiel P, Murawska-Cialowicz E, Saczko J, Kulbacka J, Gomulkiewicz A, Rossini K, Jethon Z, Carraro U, Zabel M. Source Department of Histology and Embryology, Medical University of Wroclaw, Wroclaw, Poland. mapod@hist.am.wroc.pl Abstract Regular exercise is known to improve physiological and functional capacity of many organs due to adaptive processes. We have previously shown that acute exercise in untrained rats results in apoptosis of renal tubular cells and that the apoptotic process seems to be associated with stimulation of angiotensin II, AT1 and AT2 receptors. In this study, we examined the influence of regular training on apoptosis and the role of angiotensin II receptors and antioxidant enzymes in mediating the adaptive response in renal tubular cells. We measured apoptosis, expression of AT1 and AT2 receptors, level of lipid peroxidation (TBARS) and activities of antioxidant enzymes, SOD, GPx and CAT in kidneys of sedentary rats that were exposed to acute exercise and rats that were trained for 8 weeks. In untrained animals, the acute exercise resulted in increased apoptosis and increased expression of AT1 and AT2 receptors in renal tubular cells, while in the rats exposed to the 8-week regular training, there were no changes in apoptosis nor AT1 and AT2 receptor expression as compared to the sedentary animals. The TBARS levels were significantly increased in acutely exercised rats, while in rats pre-exposed to the training they remained unchanged. The acute exercise, as well as regular training, did not change SOD, CAT or GPx activities. These findings suggested that the acute exercise-induced apoptosis in renal tubules could involve action of AT1 and AT2 receptors as well as oxidative stress, while the regular training was shown to prevent apoptosis in renal tubular cells via modulated expression of AT1 and AT2 receptors. PMID: 17102979 [PubMed - indexed for MEDLINE]
Effects of adaptive exercise on apoptosis in cells of rat renal tubuli.
ROSSINI, KATIA;CARRARO, UGO;
2007
Abstract
Eur J Appl Physiol. 2007 Feb;99(3):217-26. Epub 2006 Nov 11. Effects of adaptive exercise on apoptosis in cells of rat renal tubuli. Podhorska-Okolow M, Dziegiel P, Murawska-Cialowicz E, Saczko J, Kulbacka J, Gomulkiewicz A, Rossini K, Jethon Z, Carraro U, Zabel M. Source Department of Histology and Embryology, Medical University of Wroclaw, Wroclaw, Poland. mapod@hist.am.wroc.pl Abstract Regular exercise is known to improve physiological and functional capacity of many organs due to adaptive processes. We have previously shown that acute exercise in untrained rats results in apoptosis of renal tubular cells and that the apoptotic process seems to be associated with stimulation of angiotensin II, AT1 and AT2 receptors. In this study, we examined the influence of regular training on apoptosis and the role of angiotensin II receptors and antioxidant enzymes in mediating the adaptive response in renal tubular cells. We measured apoptosis, expression of AT1 and AT2 receptors, level of lipid peroxidation (TBARS) and activities of antioxidant enzymes, SOD, GPx and CAT in kidneys of sedentary rats that were exposed to acute exercise and rats that were trained for 8 weeks. In untrained animals, the acute exercise resulted in increased apoptosis and increased expression of AT1 and AT2 receptors in renal tubular cells, while in the rats exposed to the 8-week regular training, there were no changes in apoptosis nor AT1 and AT2 receptor expression as compared to the sedentary animals. The TBARS levels were significantly increased in acutely exercised rats, while in rats pre-exposed to the training they remained unchanged. The acute exercise, as well as regular training, did not change SOD, CAT or GPx activities. These findings suggested that the acute exercise-induced apoptosis in renal tubules could involve action of AT1 and AT2 receptors as well as oxidative stress, while the regular training was shown to prevent apoptosis in renal tubular cells via modulated expression of AT1 and AT2 receptors. PMID: 17102979 [PubMed - indexed for MEDLINE]
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